Clinical study on the effectiveness and reliability of the improved Smart Naso™ for nasalance measurement
Not Applicable
Completed
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Registration Number
- KCT0008727
- Lead Sponsor
- Jeonbuk National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
1) Men and women over 4 years old and under 80 years old
2) Those who fully understand the purpose and procedure of the study and wish to participate in the clinical study through voluntary consent
3) Subjects whose degree of hypernasal tone as a result of the VPI · Articulation Differential Test by auditory perception evaluation by a skilled speech therapist meets the criteria for each group (normal group 0, hypernasal group 1 or more)
Exclusion Criteria
1) Those who cannot maintain a sitting position for more than 15 minutes
2) Those who cannot follow the instructions of the inspector
3) Those who are judged by the researcher to be unfit to participate in clinical research due to other reasons
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method nasalance score
- Secondary Outcome Measures
Name Time Method nasalance score